Uniroid-Hc Ointment
SUMMARY OF PRODUCT CHARACTERISTICS
1 NAME OF THE MEDICINAL PRODUCT
Uniroid-HC Ointment.
2. QUALITATIVE AND QUANTITATIVE COMPOSITION
Each gram of ointment contains:
Hydrocortisone Ph.Eur. 5.0 mg
Cinchocaine Hydrochloride BP 5.0 mg
3. PHARMACEUTICAL FORM
An off-white, odourless, smooth, translucent ointment.
4 CLINICAL PARTICULARS
4.1 Therapeutic Indications
Uniroid-HC Ointment is indicated primarily for the treatment of external haemorrhoids for the short term relief of pain, irritation and associated pruritus ani. Uniroid-HC Ointment can also be used for internal haemorrhoids.
4.2 Posology and Method of Administration
Adults
Treatment with Uniroid-HC Ointment should be limited to seven days. Patients should be advised to return to their doctor if the condition persists beyond this time.
Directions for use and dosage schedule:
First wash the anal area gently with water and pat dry with cotton wool. With the finger, spread a small quantity of the ointment on the painful area without rubbing. Do not use toilet paper.
Apply the ointment twice a day (morning and evening) and after each bowel movement, or as prescribed by the doctor.
The ointment can be used internally by means of the nozzle applicator which is supplied. Insert the nozzle applicator to full extent and squeeze the tube gently from the lower end whilst withdrawing.
The nozzle applicator must be cleaned thoroughly in warm, soapy water before and after each use.
The ointment may be used separately or concurrently with the suppositories. The Elderly
Dosage modifications are not required in the elderly.
Children
Uniroid-HC Ointment is not recommended for use in children under 12 years of age unless directed by a doctor.
4.3 Contra-Indications
Known hypersensitivity to any of the constituents and to local anaesthetics. This product is contra-indicated in tuberculosis, anal thrush and most viral lesions of the skin including herpes simplex, vaccinia and varicella.
4.4 Special Warnings and Special Precautions for Use
Since the use of occlusive dressings may increase the risk of sensitivity, such dressings should be avoided. Uniroid-HC Ointment is not recommended for use in children unless recommended by a doctor.
4.5 Interactions with other Medicinal Products and other forms of Interaction
No interactions have been reported.
4.6 Pregnancy and Lactation
There is inadequate evidence of safety in human pregnancy. Topical administration of corticosteroids to pregnant animals can cause abnormalities of foetal development including cleft palate and intra-uterine growth retardation. There may, therefore, be a very small risk of such effects in the human foetus. Uniroid-HC Ointment can be used post-partum, provided the mother is not breast feeding.
4.7 Effects on Ability to Drive and Use Machines
Not applicable.
4.8 Undesirable effects
Recurrent or prolonged application may increase the risk of contact sensitisation particularly to cinchocaine. The possibility of systemic absorption should be borne in mind when prescribing preparations containing corticosteroids which can cause adrenal suppression in large doses.
Reporting of suspected adverse reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard.
4.9 Overdose
Not applicable to a product with this route of administration.
5 PHARMACOLOGICAL PROPERTIES
5.1 Pharmacodynamic Properties
Hydrocortisone
The principle pharmacological actions of hydrocortisone are on gluconeogensis, glycogen deposition, protein and calcium metabolism and inhibition of corticotrophin secretion and anti-inflammatory activity (glucocorticoid actions). When applied topically hydrocortisone causes reduction of inflammation, pruritus and exudation in disorders of the skin and perianal region.
Cinchocaine hydrochloride
Cinchocaine hydrochloride is a local anaesthetic agent and is suitable for surface or spinal anaesthesia and for relaxing sphincteric spasms. It is an anaesthetic of the amide type. It is more toxic than cocaine by local application but its local anaesthetic action is greater so it can be used in lower concentrations. Its action is more prolonged than lignocaine.
Surface or topical anaesthetics such as cinchocaine block the sensory nerve endings in the skin preventing transmissions of impulses along the nerve fibres and inhibiting depolarisation and ion-exchange. These effects are reversible. Before this blocking action can occur the lipid soluble anaesthetic base must penetrate the lipoprotein nerve sheath and the effectiveness of the anaesthetic depends on the concentration attained in the nerve fibre. The onset of action varies depending on the anaesthetic used. Cinchocaine has a rapid onset of action and is also long lasting.
5.2 Pharmacokinetic Properties
Hydrocortisone
Hydrocortisone is passed through the skin, particularly in denuded areas. About 90% of plasma hydrocortisone is bound to plasma proteins, mainly to globulin, less so to albumin. In the liver and most body tissues it is metabolised to hydrogenated and degraded forms such as tetrahydrocortisone and tetrahydrocortisol. These degraded forms are excreted in the urine. They are mainly conjugated as glucuronides. A very small proportion of unchanged hydrocortisone is excreted in the urine.
Cinchocaine hydrochloride
Most local anaesthetics such as cinchocaine hydrochloride are absorbed through damaged skin. Cinchocaine hydrochloride is an ester-type local anaesthetic. Following absorption it is hydrolysed by esterases in the plasma and liver.
5.3 Preclinical Safety Data
There are no pre-clinical data of relevance to the prescriber which are additional to that already included in other sections of the SPC.
6 PHARMACEUTICAL PARTICULARS
6.1 List of Excipients
Cetostearyl alcohol BP
White soft paraffin BP
6.2 Incompatibilities
None reported.
6.3 Shelf Life
36 months, as packaged for sale.
6.4 Special Precautions for Storage
Uniroid-HC Ointment should be stored in a cool, dry place at a temperature not exceeding 25°C (77°F).
6.5 Nature and Contents of Container
Externally white enamelled and printed; internally lacquered aluminium tube with medium density polyethylene nozzle applicator and white plug seal cap.
The product is available in tubes of 30 g and 15 g.
6.6 Instruction for Use, Handling and Disposal
Not applicable.
7 MARKETING AUTHORISATION HOLDER
Chemidex Pharma Limited
Chemidex House
Egham Business Village
Crabtree Road
Egham
Surrey
TW20 8RB
United Kingdom
8. MARKETING AUTHORISATION NUMBER
PL 17736/0001
OF
9. DATE OF FIRST AUTHORISATION/RENEWAL AUTHORISATION
3rd November 2000
10 DATE OF REVISION OF THE TEXT
24/04/2015